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1.
J Nurs Adm ; 52(6): 330-331, 2022 Jun 01.
Artículo en Inglés | MEDLINE | ID: mdl-35608976

RESUMEN

During the height of the COVID-19 pandemic, organizations had to prioritize protecting healthcare personnel (HCP) through effective communication and providing necessary personal protective equipment (PPE). Inadequate and inconsistent supply of PPE has been noted as a cause of anxiety and concern for HCPs. A pediatric hospital in the Western United States responded by developing a system of processes to protect their staff. This column describes the creation of specific COVID-19 roles to support the communication and the resourcing of PPE.


Asunto(s)
COVID-19 , Equipo de Protección Personal , Niño , Atención a la Salud , Personal de Salud , Humanos , Pandemias/prevención & control
2.
Cleft Palate Craniofac J ; 52(3): e41-6, 2015 05.
Artículo en Inglés | MEDLINE | ID: mdl-25531735

RESUMEN

OBJECTIVE: Our aim was to evaluate dental/orthodontic outcomes for patients who underwent recombinant human bone morphogenic protein (rhBMP-2) alveolar cleft repair and to examine parental satisfaction following the procedure. Design Retrospective review. Setting Tertiary children's hospital. Participants Parents, dentists, and orthodontists completed satisfaction questionnaires. Main Outcome Measures Parent, dentist, and orthodontist satisfaction with the use of rhBMP-2 in alveolar cleft repair. Results Parent response rate was 71.4% (30/42). The dentist response rate was 60% (18/30). The orthodontist response rate was 53.3% (16/30). Parent and patient satisfaction was 93.3% and 83.3%, respectively. Of dentist respondents, 55.6% reported that the bone quality and alveolar ridge mucosal repair allowed for dental treatment. Of orthodontist respondents, 87.5% reported the graft enabled treatment, and 73.3% felt the graft prevented tooth root exposure and resorption. Conclusions Parents, dentists, and orthodontists are satisfied with outcomes when rhBMP-2 is used for alveolar cleft repair. The bone formed was reported as adequate to support dental and orthodontic treatment in most cases with few complications. Because of safety concerns over the use of this product in an off-label manner, further controlled studies are warranted.


Asunto(s)
Injerto de Hueso Alveolar , Proceso Alveolar/anomalías , Proteínas Morfogenéticas Óseas/uso terapéutico , Fisura del Paladar/terapia , Odontólogos/psicología , Ortodoncistas/psicología , Padres/psicología , Niño , Femenino , Humanos , Masculino , Ortodoncia Interceptiva , Proteínas Recombinantes/uso terapéutico , Procedimientos de Cirugía Plástica , Estudios Retrospectivos , Resultado del Tratamiento
3.
Otolaryngol Head Neck Surg ; 146(3): 467-72, 2012 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-22140204

RESUMEN

OBJECTIVE: To determine benefits of early intervention in neonates with symptomatic micrognathia who underwent bilateral mandibular distraction osteogenesis within the first 90 days of life as relates to growth, need for supportive care, and further invasive procedures. STUDY DESIGN: Case series with chart review. SETTING: Tertiary care, academic children's hospital. SUBJECTS AND METHODS: Review of neonates with symptomatic micrognathia who underwent bilateral mandibular distraction osteogenesis in the past 5 years. Inclusion criteria included mandibular distraction osteogenesis performed within the first 90 days of life. Outcome measures included hospital course, growth curves, supportive home care needs, and airway at cleft repair. RESULTS: Twenty-four patients met inclusion criteria. The mean age at distraction was 30 days, and the average discharge was postoperative day 14. One patient required home oxygen, 50% were able to feed exclusively by oral diet, and no patients required tracheotomy. In addition, airway results were substantial, with 90% of patients showing objective improvement in airway grade from time of mandibular distraction to time of cleft repair. CONCLUSION: We present our initial outcomes on mandibular distraction osteogenesis in neonates with symptomatic micrognathia. Early intervention allows discharge to home with minimal supportive care needs by avoiding tracheostomy and facilitating transition to oral feeds. The airway improvement is significant and is sustained and allows for easier intubation at time of cleft repair.


Asunto(s)
Obstrucción de las Vías Aéreas/cirugía , Mandíbula/cirugía , Micrognatismo/cirugía , Osteogénesis por Distracción/métodos , Obstrucción de las Vías Aéreas/etiología , Estudios de Cohortes , Intervención Médica Temprana/métodos , Femenino , Estudios de Seguimiento , Hospitales Pediátricos , Humanos , Lactante , Recién Nacido , Masculino , Mandíbula/anomalías , Micrognatismo/complicaciones , Osteogénesis por Distracción/efectos adversos , Cuidados Posoperatorios/métodos , Complicaciones Posoperatorias/diagnóstico , Complicaciones Posoperatorias/epidemiología , Estudios Retrospectivos , Medición de Riesgo , Índice de Severidad de la Enfermedad , Factores de Tiempo , Resultado del Tratamiento
5.
Infect Control Hosp Epidemiol ; 32(8): 804-10, 2011 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-21768765

RESUMEN

OBJECTIVE: To determine the source of Burkholderia cepacia complex associated with a hospital outbreak and describe the measures taken to identify and confirm the source. SETTING: A 250-bed, tertiary care pediatric hospital in Denver, Colorado. METHODS: An epidemiologic investigation was used to identify possible causes for an apparent outbreak of B. cepacia complex in pediatric patients who had new positive cultures with this organism from December 2003 to February 2004. Chart review, microbiology reports, surgical records, site visits, literature review, staff interviews, and cultures of common products and equipment were performed to determine a source of contamination. Random amplified polymorphic DNA and pulsed-field gel electrophoresis typing, performed by 2 independent laboratories, were used for molecular typing of patient and source isolates. RESULTS: Five pediatric patients had new positive B. cepacia complex cultures from either the sinus or the respiratory tract, and all 5 patients had prior exposure to 0.05% oxymetazoline hydrochloride Major Twice-A-Day 12-hour nasal spray (Proforma, Miami, FL). Four of the 5 patients had isolates that were identical to the B. cepacia complex isolates recovered from the unopened Twice-A-Day 12-hour nasal spray. CONCLUSIONS: Intrinsic contamination of Major Twice-A-Day 12-hour nasal spray with B. cepacia complex resulted in nosocomial transmission to 4 patients at our facility and resulted in a voluntary product recall by the manufacturer. B. cepacia complex species are common contaminants of an increasing variety of nonsterile medical products. Enhanced culture techniques may be useful in evaluating possible product contamination, suggesting additional measures that should be considered to assure the safety of products that may be used in high-risk patients.


Asunto(s)
Infecciones por Burkholderia/epidemiología , Complejo Burkholderia cepacia/aislamiento & purificación , Infección Hospitalaria/epidemiología , Brotes de Enfermedades , Contaminación de Medicamentos , Control de Infecciones/métodos , Rociadores Nasales , Técnicas de Tipificación Bacteriana , Infecciones por Burkholderia/etiología , Complejo Burkholderia cepacia/clasificación , Colorado , Infección Hospitalaria/etiología , Infección Hospitalaria/microbiología , Hospitales Pediátricos , Humanos , Descongestionantes Nasales/uso terapéutico , Oximetazolina/uso terapéutico
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